Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G-Reference-Cited by-同舟云学术

Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G

Published:2014-07-23 Issue:7 Volume:9 Page:e102763
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Francis Amirtharaj,Sunitha Balaraju,Vinodh Kandavalli,Polavarapu Kiran,Katkam Shiva Krishna,Modi Sailesh,Bharath M. M. Srinivas,Gayathri Narayanappa,Nalini Atchayaram,Thangaraj Kumarasamy

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference35 articles.

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2. The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12;ES Moreira;Am J Hum Genet,1997

3. G.P.8.15 Limb girdle muscular dystrophy 2G and novel TCAP mutations in ethnic Chinese;W Yee;Neuromuscular disorders: NMD,2007

4. Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient;M Olive;Neuromuscul Disord,2008

5. Limb-girdle muscular dystrophy in a Portuguese patient caused by a mutation in the telethonin gene;L Negrao;Acta Myol,2010

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